淖毛湖次烟煤的热溶及热溶物的催化加氢转化

Thermal dissolution of Naomaohu sub-bituminous coal and catalytic hydroconversion of its soluble portions

  • 摘要: 采用等体积甲醇/甲苯混合溶剂对淖毛湖次烟煤(NMH)进行热溶得到热溶物和热溶残渣(RTD),利用Co/C@N-700催化剂催化320 ℃热溶物(SP320)加氢转化得到CSP320。利用气相色谱质谱联用仪(GC/MS)分析了SP320催化加氢前后的组成和结构特征,利用傅里叶变换红外光谱(FT-IR)、热重以及固体 13C核磁共振(13C NMR)分析了NMH和RTD的热解反应性和结构特征。热溶物收率随温度升高而增加,320 ℃达到最大值(36.46%)。GC/MS分析表明,烷烃、芳烃和酚类是SP320中的主要族组分,相对含量分别为45.45%、18.03%和24.75%;经催化加氢后芳烃和酚类相对含量分别降低至3.86%和13.6%,烷烃和醇类含量分别提高至66.99%和9.36%,其中,环烷烃由8种增加至24种,这说明Co/C@N-700对SP320中芳烃和酚类加氢转化具有较高活性。与NMH相比,RTD具有较高的热稳定性,骨架结构中芳香碳含量较高,而羰基碳含量较低;RTD的FT-IR谱图中O−H、−CH2−、C=O以及C−O−C对应的吸收峰强度显著减弱,芳香C=C的吸收峰强度明显增强。

     

    Abstract: Naomaohu sub-bituminous coal (NMH) was thermally dissolved in isometric methanol/toluene mixed solvent affording soluble portions (SPs) and thermal dissolution residues (RTD), then hydroconversion of SP320 was catalyzed over Co/C@N-700 catalyst affording CSP320. The composition and structural characteristics of SP320 before and after catalytic hydroconversion were analyzed with a gas chromatograph/mass spectrometer (GC/MS), and pyrolysis reactivity and structural characteristics of NMH and RTD were characterized with Fourier transform-infrared spectroscopy (FT-IR), thermogravimetry, as well as solid state 13C nuclear magnetic resonance (13C NMR). The SPs yields increase with increasing temperature, and reach a maximum (36.46%) at 320 oC. GC/MS analysis shows that SP320 are mainly composed of alkanes, phenols and arenes, and their relative contents are 45.45%, 18.03% and 24.75%, respectively. After catalytic hydroconversion, relative contents of arenes and phenols in CSP320 decrease to 3.86% and 13.6%, respectively, while those of alkanes and alcohols increase to 66.99% and 9.36%, respectively, and kinds of cycloalkanes increase from 8 to 24. These results indicate that arenes and phenols in SP320 could be hydrogenated into alkanes and alcohols catalyzed by Co/C@N-700. Compared to NMH, RTD possesses higher thermal stability, more aromatic carbons, and less carbonyl carbons in its skeleton structure. In addition, intensity of adsorption peaks attributed to O−H, −CH2−, C=O and C−O−C in the FT-IR spectrum of RTD are weaker, while adsorption peaks assigned to aromatic C=C are stronger than those of NMH.

     

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